http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2081891-C

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-68
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filingDate 1991-05-01^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-03-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_753762b254eb0e4d7ab5c5df5648db1e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2eac455f4fc1c7ec41617ec9988265b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe25a5bbcb621eebecf50dd9bea2dfd7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63c9faaf1b47072436e6e93671bc01a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4948628245154d20e0bca8ea1330d6b0
publicationDate 1999-03-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2081891-C
titleOfInvention Quinolizinone type compounds
abstract Novel compounds are disclosed having formula (I) as well as pharmaceutically acceptable salts, esters and amides thereof, wherein R1 is selected from (a) loweralkyl, (b) loweralkenyl, (c) halo(loweralkyl), (d) loweralkoxy, (e) cycloalkyl of from 3 to 8 carbons (f) phenyl, (g) halo, (h) cyano, (i) nitro, (j) bicycloalkyl, (k) loweralkynyl, (l) alkoxycarbonyl, (m) nitrogen-containing aromatic heterocycle and (n) a group of the formula -NR7R8; R2 is selected from the group containing of halogen, loweralkoxy, carbocyclic aryloxy or carbocyclic aryl(loweralkyl)oxy, loweralkyl, loweralkenyl, cycloalkyl of from 3 to 8 carbons, cycloalkenyl of from 4 to 8 carbons, carbocyclic aryl(loweralkyl), cycloalkyl(loweralkyl), phenyl, amino, (loweralkyl)amino, carbocyclic aryl(loweralkyl)amino, hydroxy-substituted (loweralkyl)amino, nitrogen-containing aromatic heterocycle, bicyclic nitrogen-containing heterocycle and nitrogen-containing heterocycle having formula (II), wherein x is 0 to 3; R9 is selected from (a)-(CH2)m-, wherein m is 1, 2 or 3, and (b) -(CH2)n R10(CH,)p-, wherein R10 is selected from S, O and N, n is 1 or 2, and p is 1 or 2: and Y is a non-hydrogen substituent independently selected from loweralkyl, halo(loweralkyl), loweralkoxy, hydroxy-substituted loweralkyl, hydroxy, amino(loweralkyl), halogen and a group having the formula -NR11R12; R3 is hydrogen, halogen or loweralkoxy; R4 is selected from the group consisting of hydrogen loweralkyl, a pharmaceutically acceptable cation and a prodrug ester group: R5 is selected from the group consisting of hydrogen halogen, hydroxy, loweralkyl, halo(loweralkyl), loweralkoxy and a group having the formula -NR13R14; and A is N or CR6, wherein R6 is selected from hydrogen, halogen, loweralkyl. halo(loweralkyl), hydroxy-substituted loweralkyl, loweralkoxy(loweralkyl), loweralkoxy and amino(loweralkyl) or, alternatively, R1 and R6, taken together with the atoms to which they are attached form a 6-membered saturated ring which may contain an oxygen or a sulfur atom and which may be substituted with loweralkyl; with the proviso that when R5 is hydrogen and A is CH then either (a) R1 is NR7R8, or (b) R2 is a group having formula (III), wherein x is 1-3 and R9 and Y are as defined above.
priorityDate 1990-05-02^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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